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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251015Generated: October 26, 2026

tert-butyl N-(4-aminobutyl)carbamate → [4-(1-Pyrazin-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/251015

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantAcetylpyrazineHCID 30914—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product[4-(1-Pyrazin-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl esterHCID 6727261691%

Reaction Steps

Using General Procedure B: Reaction of (4-amino-butyl)-carbamic acid tert-butyl ester and 2-acetyl pyrazine in MeOH with NaBH4 gave [4-(1-pyrazin-2-yl-ethylamino)-butyl]-carbamic acid tert-butyl ester (294 mg, 91%) as a colorless oil. 1H NMR (CDCl3) δ 1.44 (s, 9H), 1.50-1.57 (m, 4H), 1.59 (d, 3H, J=6.6 Hz), 2.38-2.43 (m, 1H), 2.51-2.59 (m, 1H), 3.08-3.14 (m, 2H), 3.08 (m, 2H), 3.91 (d, 1H, J=6.7 Hz), 4.72 (bs, 1H), 8.45 (d, 1H, J=2.5 Hz), 8.53 (d, 1H, J=2.6 Hz), 8.60 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863293B2
Source datasetuspto-grants-2011_01
ORD IDord-4d6ae50c524e4a61ad21449c548a6123
Source noteuspto-grants-2011_01